Storage: 2-8°C
UNSPSC Code: 12352200
RIDADR: NONH for all modes of transport
Application:
Use Anti-Digoxigenin-Rhodamine, Fab fragments for the detection of digoxigenin-labeled compounds using:
• Digoxigenin-labeled sugars in glycoconjugate research
• Fluorescent in situ hybridization (FISH)
• Immunohistocytochemistry
• In situ hybridization
• DNA fiber assay
General description:
Fab fragments from polyclonal anti-digoxigenin antibodies, conjugated to rhodamine.
Other Notes:
For life science research only. Not for use in diagnostic procedures.
Preparation Note:
After immunization with digoxigenin, sheep IgG was purified by ion-exchange chromatography, and the specific IgG was isolated by immunosorption. The Fab fragments obtained by papain digestion were purified by gel filtration, conjugated to the specific label, and stabilized in buffer.
Working concentration: Working concentration of conjugate depends on application and substrate. The following concentrations should be taken as a guideline: Detection of digoxigenin-labeled sugars in glycoconjugates: 20 to 50 μg/ml
• Fluorescent in situ hybridization (FISH): 1 to 20 μg/ml
• Immunohistocytochemistry: 20 to 50 μg/ml
• In situ hybridization: 20 to 50 μg/ml
Working solution: PBS, 0.5% bovine serum albumin (w/v), pH 7.4.
1% Blocking reagent (w/v), 1 to 5% heat inactivated fetal calf serum (v/v) or sheep normal serum can be used for reduction of unspecific binding. Furthermore pH can be increased up to pH 8.5 to 9.0.
Storage conditions (working solution): Always prepare fresh!
Reconstitution:
Add 1 ml double-distilled water to a final concentration of 200 μg/ml.
Specificity:
Polyclonal antibodies from sheep show 100% reactivity with digoxigenin and digoxin, but no cross-reactivity with other steroids, such as human estrogens (e.g., estradiol) or androgens (e.g., testosterone).